A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606546



Internal ID21554851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42956082..42956082hg38UCSC Ensembl
chrX:42815331..42815331hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167264
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606546
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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